Table Of ContentBULLETIN DE L'INSTITUT ROYAL DES SCIENCES NATURELLES DE BELGIQUE, BIOLOGIE, 68: I 11-122, 1998
BULLETIN VAN HET KONINKLIJK BELGISCH fNSTITUUT VOOR NATUURWETENSCHAPPEN, BIOLOGIE, 68: 111-122, 1998
A new thalassocypridine genus (Crustacea, Ostracoda) from brackish waters
in the Indian and Pacific Oceans, with the description of a new species
by Karel WOUTERS
Abstract tations and to unsolved synonymies. Since several years
I have been working on this group in an attempt to under
Mangalocypria, a new genus of the tribe Thalassocypridini, is stand the complicated systematical context of paracypridine
described, with a new species, and two previously described and thalassocypridine genera. The existing descriptions
species, from Papua New Guinea, the Comoros and Indonesia.
and figures are sometimes too vague or incomplete for
The new genus has a remarkable set of characters separating
taxonomical interpretation, and therefore restudy of the
it from other members in the tribe: thin-shelled, translucent and
type material, if available and sufficiently well preserved,
smooth valves, V-process of lower lip developed as a rake, and
is certainly necessary. To solve some of the long standing
postero- distal claw of furca fixed to·shaft without a joint. The
taxonomical problems in this group, the study of the type
affinities of Mangalocypria gen. nov. with other genera is
material may well be insufficient, and the presence of
discussed, and some taxonomical problems in the tribe
new material is essential.
Thalassocypridini are commented upon. The diagnostic value
of incompletely differentiated Zenker organs of premature males Recently collected material from Papua New Guinea, the
is discussed. Comoros and Indonesia, containing thalassocypridines,
appeared to be very useful in this respect, and was used
Key-words: Ostracoda, meiofauna, taxonomy, new genus, Indian in the present study. Detailed analysis of the morphology
Ocean, Pacific Ocean. of the valves, but especially of the soft parts led to the
description of new features which can be used in unrav
elling the taxonomical confusion in the thalassocypridines.
Resume
The logical consequence of this all was that a new genus
had to be described.
Mangalocypria, un nouveau genre du tribu Thalassocypridini
The material used in this study is deposited in the ostracod
est decrit, avec une nouvelle espece et deux especes connues,
collection of the Royal Belgian Institute of Natural
de Ia Papouasie Nouvelle-Guinee, des Co mores et de l 'Indonesie.
Sciences, Brussels.
Le nouveau genre se distingue par un ensemble remarquable
de caracteres qui sont absents chez d'autres membres du tribu:
valves minces, translucides et lisses, le rameau V de Ia levre Taxonomic account
inferieure est developpee en forme de rateau, et Ia griffe postero
distale de Ia furca et fixee au branche sans articulation.
Order Podocopida G.W. MOLLER, 1894
Les relations de Mangalocypris avec d'autres genres et quelques
Suborder Podocopina SARS, 1866
problemes taxonomiques dans le tribu des Thalassocypridini
Superfamily Cypridoidea BAIRD, 1845
sont discutes. La valeur diagnostique des organes de Zenker
Family Candonidae KAUFMANN, 1900
incompletement differencies chez des males prematures est
Subfamily Paracypridinae SARS, 1923
discutee.
Tribe Thalassocypridini HARTMANN & PURl, 1974
Mots-cles: Ostracoda, meiofaune, taxonomie, nouveau genre,
Ocean Jndien, Ocean Pacifique.
Genus Mangalocypria gen. nov.
DERIVATION OF NAME
Introduction
From 'Mangal' = mangrove formation, and the suffix
The tribe Thalassocypridini is a poorly known group of
-cypria (gender feminine).
brackish and marine cypridacean ostracods. Several genera
in the tribe are ill-defined, and need to be redescribed.
This situation has led in the past to conflicting interpre-
TYPE SPECIES
Leopold Jli Biological Station Laing Island, Contribution N° 351 Mangalocypria appendix sp. nov. (here designated).
112 K. WOUTERS
12
Figs 1-17. - Mangalocypria appendix gen. et sp. nov., Papua New Guinea, Madang Province.
I. Right valve, male, internal view, holotype (O.C. 2176). 2. Antennule, male, holotype. 3. Antenna, male, holotype.
4. Mandibular palp, male, paratype (O.C. 2177). 5. Mandibular epipodite, male, holotype. 6. Mandible, male, paratype
(O.C. 2177). 7-8. Clasping organs, male, holotype. 9. Maxillule, male, holotype. I 0. Second leg, male, holotype.
II. Furca, male, holotype. 12. Furcal attachment, male, holotype. 13. Zenker organ, male, holotype. 14. Ze11ker organ,
premature male, paratype (O.C. 2177). 15. Male copulatory organ, holotype. 16. Third leg, cleaning limb, male,
holotype. 17. Lower lip, female (O.C. 2185).
A new thalassocypridine genus (Crustacea, Ostracoda) 113
OTHER SPECIES 3246, 3252, 3253, 3257 and 3259), O.C. 2198, 2190,
2191, 2192, 2195.
Mangalocypria eleotridis (HARDING, 1962) nov. comb. Note: salinities measured with a salinity refractometer.
Mangalocypria africana (HARTMANN, 1974) nov. comb.
DIAGNOSIS
DIAGNOSIS
Medium-sized valves, with evenly convex dorsal margin;
Thin-shelled, fragile, translucent and smooth valves, with Carapace spindle-shaped in dorsal view, with greatest
broadly and regularly rounded anterior and posterior width in the middle; Rome organ with distal expansion;
margins; copulatory appendage with three distal lobes; natatory setae of antenna reaching just beyond tip of
V-process of lower lip developed as a rake; postero-distal distal claws; distal setae of third and fourth segment of
claw of furca fixed to the shaft without a joint. second leg short; dorsal lobe of copulatory appendage
Discussion: see below. triangular, ventral lobe a narrowly curved hook.
Mangalocypria appendix sp. nov. DESCRIPTION
Figs 1-17, 45-50, 57
Valves (Figs I, 45-50, 57) thin-shelled, fragile, translucent
DERlVATION OF NAME: Latin appendix, because of the and very smooth, bean-shaped; anterior margin broadly
rounded; dorsal margin regularly convex: ventral margin
large expansion on the Rome-organ (used as a noun in
straight; transition between anterior, dorsal, posterior and
apposition).
ventral margins smooth, without angles; greatest height
located near mid-length; carapace in dorsal view spindle
TYPE LOCALITY: Papua New Guinea, Madang Province,
shaped, with pointed extremities; greatest width in the
Hansa Bay, Sisimangun village, pond on the beach, NW
middle. Sexual dimorphism: female valves about I 0%
of the village. Salinity: 4 g )·1; leg.: K. Wouters, 27 May
larger than males. Anterior inner lamella moderately wide,
1982 (station 323 7).
posterior one narrow; zone of concrescence narrow; few,
short, fine and hardly visible marginal pore canals; anterior
vestibulum deep and open, posterior one narrow; muscle
HOLOTYPE
scar pattern consisting of a curved anterior row of four
scars and two small scars behind this row; hinge adont.
A dissected male with valves stored dry (O.C. 2176a)
Antennule (Fig. 2) fairly slender, seven podomeres
and soft parts preserved in a sealed glycerine preparation
separate; segments 1 and 2 fused; setae long and slender;
(O.C. 2176b).
Rome-organ large, with remarkable distal expansion.
Antenna (Fig. 3): podomeres 4 and 5 distinctly divided
in males, but fused in females; long swimming setae
PARAT YPES
reaching slightly beyond the tip of the terminal claw; Y
aesthetasc long and slender, with a median suture.
Three females and three males, dissected and stored as
Mandibula (Figs 4-6): vibratory plate of palp with one
the holotype (O.C. 2177-2182).
short and seven long feathered setae: molar teeth bifid
or trifid.
Maxillule (Fig. 9): with. a two-segmented short palp;
OTHER MATERIAL
terminal segment subrectangular; vibratory plate with six
mouthward-directed "Strahlen".
All material originates from northern Papua New Guinea,
First leg (Figs 7-8): male clasping apparatus with subrec
Madang Province.
tangular body (first segment), and sigmoid terminal hook
Five microscopical preparations, River Boroi and Nubia
(second segment); pegs short and stout.
Mission, salinities ranging from 1 to 14 g J·1(Leg.:
Second leg (Fig. 10 ): five-segmented, with a long and
K. WouTERS, 21 May, 26 May and 17 June 1982, stations
slender curved terminal claw; terminal segment very small.
3180, 3223 and 3371) (O.C. 2183-2187).
Third leg (cleaning limb )(Fig. 16): five-segmented; penul
Seventeen specimens preserved in ethanol, from tlu-ee
timate segment not divided; two short terminal setae, and
samples in the River Boroi, between Boroi Village and
one long two-segmented reflexed seta, with terminal
Bak Village, salinities ranging from 6 to 16 (Leg.: setules arranged in a comb-like pattern; joint between
K. WOUTERS, 26 May 1982, stations 3219, 3222 and the two segments of the reflexed seta in the middle.
3223), O.C. 2188, 2193 and 2194. Furca (Fig. 11): large and slightly curved; one short distal
Thirteen specimens preserved in ethanol, from five seta and two large serrate terminal claws; posterior claw
samples in the River Aw ar, salinities 1, 4, 6, 8 and 11 g connected to shaft without a joint; two short and thin
J·I respectively (Leg.: K. WOUTERS, 28 May 1982, stations posterior setae; posterior part of distal half of shaft set
114 K. WOUTERS II
Figs 18-25. - Mangalocypria czji-icana (HARTMANN, 1974), The Comoros, Grande Comore, Lac Sale, S. of Mitsiamouli.
18. Right valve, male, internal view (O.C. 2198). 19. Left valve, male, internal view (O.C. 2189). 20. Antenna,
male (O.C. 2202). 21. Antennule, male (O.C. 2196). 22. Mandibular palp, male (O.C. 2198). 23. Mandibular epipodite,
male (O.C. 2197). 24. Mandibula, female (O.C. 2200). 25. Lower lip, male (O.C. 2196).
A new thalassocypridine genus (Crustacea, Ostracoda) 115
with numerous very small spinules arranged in indistinct M. appendix. In dorsal view, the greatest width is situated
rows. in the middle in M. appendix and clearly in front of the
Furcal attachment (Fig. 12) simple, with slightly curved middle in M. aji·icana. M. eleotridis is very closely related
central axis and dorsal branch semi-circularly curved in with M. appendix. The expansion on the Rome organ,
posterior direction. and the narrowly curved hook of the ventral lobe of the
Copulatory appendage (Fig. 15) with three lobes: a small copulatory appendage in M. appendix, however, allow an
triangular dorsal lobe (a), a larger triangular median lobe easy distinction between the two species. According to
(b) and a narrowly curved hook-like ventral lobe (c). the measures given by Harding ( 1962) M. eleotridis is a
Lower lip (Fig. 17) with V-process (sensu SCI-!ULZ, 1976)
markedly larger species.
developed as a rake, resembling the T-process; the latter
is set with teeth as in many other ostracods; teeth on the
V-process slightly smaller than those on the T-process; Mangalocypria africana (HARTMANN, 1974) nov. comb.
about thirteen teeth on each of the four processes. Figs 18-34, 51-56, 58
Zenker organ (Figs 13, 14): with five rosettes and a large
and spherically enlarged entrance; spines on rosettes absent Thalassocypria africana n. sp., HARTMANN, 1974, p. 364-365,
in some specimens (Fig. 14). The absence of spines was Plate 145, Figs I 006-I 0 I 4.
already described in other ostracods, including
Thalassocypridini. Since in our matclial both spine-bearing
and spine-lacking specimens occur together, the latter TYPE LOCALITY
phenomenon is interpreted as being the premature state
(see general discussion). Costa do Sol mud flat, north of Louren<;o Marques (=
Maputo), Mozambique.
Dimensions
Holotype: length 0.73 mm; height 0.37 mm.
Paratypes: length 0.72 - 0.82 mm; height 0.35 - 0.42 mm.
MATERIAL USED FOR REDECRIPTTON
I. The Comoros, Grande Comore, Lac Sale, South of
OCCURRENCE Mitsiamouli. Leg. J.-L. KENNES (Expedition Karthala 81),
28 July 1981 (stations I and 4): 3 dissected males and
The new species was found in Northern Papua New
3 dissected females (O.C. 2196-2202), and 70 specimens
Guinea, Madang Province. The type locality is a brackish
preserved in ethanol (O.C. 2209).
beach pond near the village of Sisimangun, with stagnant
2. Papua New Guinea, southern coast, Motupore Island,
water and fluctuating salinities. When the material was
near Port Moresby, mangrove along NE beach of the
collected, a salinity of 4 g J·' was measured. All other
island, narrow strip of mangroves, in open connection
localities are situated in the same region as the type
with the sea; salinity not measured, but nearly marine;
locality and represent different types of habitats: a large
material collected at the high water level (pers. comm.
tidal river (Boroi), a small tidal river (Awar) and a ditch
FR. FIERS). Leg. FR. F!ERS, 21 November 1986 (station
(Nubia). In the studied localities, measured salinities
86): 2 dissected males and I dissected female (O.C. 2203-
ranged from I to 16 g t·'. Mangalocypria appendix sp.
2205).
nov. can therefore be described as an oligo- to mesohaline
3. Indonesia, Northern Bali, large sand flat between Merta
species. It was found living together with, among others,
Sari and Serangan Island, mangrove formation; salinity
Dolerocypria taalensis TRESSLER, 1937, Renaudcypris wolffi
25 g 1·'. Leg. FR. FrERS, 30 November 1986 (station 101):
(HARDING, 1962), Mungava munda HARDING, 1962 and
I dissected male (O.C. 2206).
Paracypria sp.
4. Indonesia, Sulawesi, Panikiang Island, about I 00 Km
N of Ujung Pandang, mangrove. Leg.: CL. MASS!N, 29
DIFFERENTIAL DIAGNOSIS August 1994 (Station 44): I dissected male, and I whole
carapace (O.C. 2207-2208).
Mangalocypria appendix can be easily distinguished from
the two other species, M. africana and M. eleotridis, by
the presence of a large expansion on the Rome organ. DIAGNOSIS
From M. a.fricana it differs by the length of the natatory
setae (longer in M. africana) and by the morphology of Medium-sized valves, with postero-dorsal margin tapering
the lobes of the copulatory appendage. In M. africana towards posterior end; carapace spindle-shaped in dorsal
the dorsal lobe is rounded whereas in M. appendix it is view, with greatest width in front of the middle; Rome
triangular. The distal setae on the third and fourth segment organ without distal expansion; natatory setae of antenna
of the second leg are much longer in M. africana. long; distal setae of third and fourth segment of the
Furthermore the dorsal margin, especially in the right second leg long; dorsal lobe of copulatory appendage
valve, is tapering in M. aji·icana, and evenly curved in rounded, ventral lobe weakly developed and narrow.
''
116 K. WOUTERS
26
b
29
50J
fm
50
fm
50fm
Figs 26-34. - Manga/ocypria africana (HARTMANN, 1974), The Comoros, Grande Comore, Lac Sale, S. of Mitsiamouli.
26. Maxillule, male (O.C. 2196). 27-28. Male clasping organs (O.C. 2197). 29. Second leg, male (O.C. 2187). 30
Male copulatory organ (O.C. 2198). 31. Third leg, cleaning limb, male (O.C. 2196). 32. Furca, male (O.C. 2198).
33. Furcal attachment , male (O.C. 2198). 34. Zenker organ, male (O.C. 2202).
A new thalassocypridine genus (Crustacea, Ostracoda) 117
50 50
I'm jim
43
50pm
Figs 35-44. - Mangalocypria eleotridis (HARDING, 1962). Holotype (male), Solomon Islands, Rennell Island, Lake Tegano, Niupani
(Zoologisk Museum Copenhagen).
35. Antennule. 36. Antenna. 37. Third leg, cleaning limb. 38. Mandibula. 39. Copulatory appendage. 40. Furca. 4!.
Maxilulle. 42-43. Clasping organs. 44. Second leg.
,,
118 K. WOUTERS
ADDITIONAL REDESCRIPTION formation on Motupore Island (S. Papua New Guinea).
The two measured salinity values, and the nearly marine
Valves (Figs 18, 19) thin, translucent and smooth; dorsal condition of the mangrove formation on Motupore Island
margin convex; posterior margin of left valve narrowly suggest that M. afi'icana is a polyhaline, perhaps even a
rounded; maximal height situated in front of the middle; mixoeuhaline species, in contrast with M. appendLr: and
sexual dimorphism indistinct: male and female valves M. eleotridis, which can be described as an oligo- to
with the same lengths, but female valves higher. Carapace mesohaline species.
spindle-shaped, with greatest width situated somewhat in
front of the middle. Anterior and posterior inner lamellae
moderately wide; zone of concrescence narrow, with few Mangalocypria eleotridis (HARDING, 1962) nov. comb.
short marginal pore canals. Muscle scar pattern consisting (Figs 35-44)
of a curved anterior row of four scars and two small
scars behind this row. Paracypria eleotridis n.sp., HARDING, 1962, p. 56-58, Figs 25-35.
Antennule (Fig. 21 ): with Rome organ well developed,
but without distal expansion.
Antenna (Fig. 20): slender, with long podomeres; natatory TYPE LOCALITY
setae reaching about 35 % beyond the tip of the terminal
claws. Solomon Islands, Renne!! Island, Lake Tegano (= Te
Mandible and maxillule (Figs 22-24, 26) without special Nggano), from the stomach content of the fish Eleotris
features. fitsca (BLOCH & SCHNEIDER). Collected during the Danish
First leg (Figs 27, 28): male clasping organ with subrec Rennell Expedition in 1965 (see WOLFF, 1968).
tangular first segment and large terminal hook (second
segment).
Second leg (Fig. 29): five-segmented; distal setae of third MATERIAL USED FOR DESCRIPTION
and fourth segments long.
Third leg (cleaning limb )(Fig. 31 ): reflexed seta two The original description of the species was based on a
segmented; joint between the two segments beyond the single specimen, the holotype. It consists of a broken shell
middle. preserved in alcohol and the appendages mounted on a
Furca (Fig. 32) almost straight, with relatively short serrate slide. I had the microscopical slide with the appendages
terminal claws. on loan from the Zoological Museum Copenhagen.
Furcal attachment (Fig. 33) with slightly curved central No other specimens of this species are known.
axis and strongly curved dorsal branch.
Copulatory appendage (Fig. 30) with three lobes: a distally
rounded dorsal lobe (a), a large obliquely pointed trian DIAGNOSIS
gular median lobe (b), and a narrow and curved ventral
lobe (c). Large valves; Rome organ without distal expansion;
Lower lip (Fig. 25) with V-process (sensu SCHULZ, 1976) natatory setae of antenna reaching slightly beyond tip of
developed as a rake; teeth on the V-process markedly claws; distal setae of third and fourth segment of second
smaller than those on the T-process; thirteen teeth on the leg short; hook of male clasping apparatus short; dorsal
T-process, and 13-16 on the V-process. lobe of copulatory appendage triangular, ventral lobe
Zenker organ (Fig. 34) with five rosettes and a large strongly developed and widely curved.
spherical entrance.
Dimensions
Holotype (HARTMANN, 1975, p. 365): length 0.75 mm, ADDITIONAL DESCRIPTION OF HOLOTYPE
height 0.36 mm.
Material from the Comoros and Indonesia: length 0.71 - Valves: there is no further information on valve
0.81 mm, length 0.35 - 0.41 mm. morphology (not seen).
Antenna (Fig. 35): with very small Rome-organ, the latter
without distal expansion.
OCCURRENCE Antenna (Fig. 36): natatory setae reaching just beyond
the tip of the terminal claws.
Mangalocypria africana was originally described from a Mandible and maxillule (Figs 38, 41) without special
mud flat, with Zostera, near Louren<;o Marques (Matupo, features.
Mozambique), with a salinity of32 g I-1• HARTMANN (1974) First leg (Figs 42, 43): subrectangular first segment, with
indicates that the salinity of the mud flat is probably short and broad terminal hook (second segment).
strongly fluctuating during the rainy season. The species Second leg (Fig. 44): distal setae of third and fourth
is now reported to have a much wider distribution and segment short.
was found in a saline lake in the Comoros, a mangrove Third leg (Fig. 37): reflexed seta two-segmented; this seta
formation in Sulawesi, a sand flat in Bali, and a mangrove is broken, but the joint between the two segments is
A new thalassocypridine genus (Crustacea, Ostracoda) 119
probably situated near or even somewhat in front of the underlined that between closely related genera "homeo
middle. morphic confusion can only be avoided by looking for
Furca (Fig. 40): long, almost straight, and with long the apomorphic details in valves and soft parts which
serrate terminal claws. distinguish them from each other". The new genus
Furcal attachment: not found. described here is based on new material, and on
Copulatory appendage (Fig. 39): with three lobes: a trian comparison with type specimens of some thalassocypidine
gular, distally pointed dorsal lobe (a), a large truncate species. From this detailed comparison it appeared that
median lobe (b), and a widely curved hook-like ventral it shows a unique set of characters, warranting the creation
lobe (c). It is not excluded that the median lobe (b) is of a new genus.
actually triangular, because in the preparation this lobe
gives the impression to be folded.
Lower lip: no further information. DIFFERENTIAL DIAGNOSIS
Zenker organ: see fig. 35 of HARDING (1962).
The new genus Mangalocypria is characterised by thin
Dimensions shelled, fragile, translucent and smooth valves, with
Holotype (HARDING, 1962, p. 56): length 0.98 mm, height broadly and regularly rounded anterior and posterior
0.44. margins; copulatory appendage with three distal lobes;
This is markedly larger that the two other species described V-process of lower lip developed as a rake; postero-distal
here, but these measurements could not be checked. claw of furca fixed to the shaft without a joint.
The combination of these characters has not been seen
elsewhere in the Thalassocypridini. The rounded shape
OCCURRENCE of the valves is reminiscent of some Mungava-species.
The genus Mungava, however, differs in many aspects,
The species is known from the type locality, Lake Tegano, both of the valves and the appendages (see WOUTERS,
the largest brackish lake in the Pacific only. The lake has 1987, MADDOCKS, 1992).
a salinity of 4.5 g (·I (HARDING, 1962). The most important characteristic of the new genus is
in the structure of the lower lip. In Mangalocypria gen.
nov., the V-process is developed as a rake, giving the
General discussion lower lip the appearance of a double rake. This feature
is unique, has not yet been observed in other genera of
TAXONOMY the tribe Thalassocypridini, and not even in other ostracod
(sub-)families. In Parapontoparta and Paracypria, the two
The tribe Thalassocypridini is a poorly understood group thalassocypridine genera that are closest to Mangalocypria,
of marine and brackish water cypridaceans. It presently the V-process is a blunt, relatively short extremity, without
consists of six genera: Dolerocypria TRESSLER, 193 7, the development of a rake. For this purpose, I compared
Mungava, HARDING, 1962, Paracypria SARS, 1905, the type specimen of Parapontoparta arcuata HARTMANN,
Pontoparta VAVRA, 1901, Parapontoparta HARTMANN, 1955 1955 (Z.I.M., n° 27455), and
and Thalassocypria HARTMANN, 1957. different species of the genus Paracypria, including
The genera Dolerocypria and Mungava are relatively well paratypes of Paracypria inujimensis (OKUBO, 1980) nov.
known. Paracypria is a widely distributed genus with comb. (described as Thalassocypria) in the collections
numerous species, which can be divided in at least three of the Royal Belgian Institute of Natural Sciences,
species groups around P tenuis SARS 1905, P marybor Brussels.
oughensis HARTMANN, 1981 and P minuta McKENZIE 1968 Another remarkable feature is the presence of a fixed
resp. The genus Pontoparta remains ill-defined. This genus postero-dorsal furcal claw. This has, until now, not yet
has as type species P rara VAVRA, 190 I, described on been observed in any other cypridacean ostracod.
the basis of a single female type specimen, which is Comparison with species in Paracypria and Parapontoparta
moreover lost. Some other species assigned to Pontoparta revealed that in these genera the postero-distal claw is
probably do not belong there. The genera Parapontoparta not fixed, but attached to the furca by means of a joint.
and Thalassocypria need to be redescribed to establish Although this may seem to be an unimportant character,
their affinities with other genera and particularly with it is interesting to note that all three species here referred
Paracypria. to the new genus, clearly shear this feature as a synapo
One could raise the question why a new genus is necessary morphy.
in a subfamily where there is so much taxonomical This illustrates that detailed analysis of the soft parts can
confusion. MADDOCKS (1992, .p. 2) already argued that a reveal new features, which are useful in unravelling
conservative strategy for the present, should be "to forego complex taxonomical relationships. The complete
new taxa until substantially more evidence is available", description and/or figuration of valve and soft part
and McKENZIE (1982, p; 417), when discussing problems characters therefore should be standard procedure when
in the Paracypridini, a tribe where the taxonomical dealing with new taxa, even when at the time of
imbroglio is even greater than in the Thalassocypridini, description certain features do not seem particularly
''
120 K. WOUTERS
Figs 45-50 and 57. Mangalocypria appendix gen. et sp. nov. 45-48 from the type locality, Sisimangun (Papua N.G.); 49, 50 and
57 from River Boroi (Papua N.G.).
45. Left valve, male, lateral view, holotype (O.C. 2176). 46. Right valve, male, lateral view, para type (O.C. 2180). 47. Left valve,
female, lateral view, paratype (O.C. 2182). 48. Right valve, female, lateral view, paratype (O.C. 2182). 49. Right valve, male,
internal view (O.C. 2183). 50. Left valve, male, internal view (O.C. 2183). 57. Carapace, male, dorsal view (left = anterior)(O.C.
2187).
Figs 51-56 and 58. Mangalocypria africana (HARTMANN, 1974). 51-56 from the Comoros, Grande Comore, Lac Sale, S. of
Mitsiamouli. 58 from Indonesia, Sulawesi, Panikiang Island.
51. Left valve, male, lateral view (O.C. 2198). 52. Right valve, male, lateral view (O.C. 2198). 53. Left valve, female, lateral
view (O.C. 2199). 54. Right valve, female, lateral view (O.C. 2199). 55. Right valve, male, internal view (O.C. 2202). 56. Left
valve, male, internal view (O.C. 2202). 58. Carapace, male, dorsal view (left = anterior) (O.C. 2208).
